ChainFor™
by Vitrosens Biotechnology Inc. 134 variants
Part of a family of 6 devices: see the family page
Ref PCR167Model CFP167P50
ChainFor™ (PCR167) is a device classified as IVD General (EU), Class C (EU) made by Vitrosens Biotechnology Inc., registered in EUDAMED on 5 Aug 2026 (Basic UDI-DI B-08684595033296), active as of 24 Oct 2026.
Active
CE IVDR CE IVDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR | NumberB-08684595033296 08684595033296 | Date5 Aug 2026 | StatusActive |
| European Union | CE/IVDD | NumberB-08684595033296 08684595033296 | Date5 Aug 2026 | StatusActive |
Official records
- EUDAMED public site B-08684595033296
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDR, CE/IVDD Active
Specification
- Device name
- CT/NG/MG/TP Genotyping qPCR Kit
- Model / reference
- CFP167P50, PCR167
- Primary DI / UDI-DI
- 08684595033296
- Basic UDI-DI
- B-08684595033296, 868521452PCR167GL
- EMDN code
- W0105070501 Stis / stds (c.trachomatis, n.gonorrhoeae ,m.genitalium, t.vaginalis, ureaplasma spp….) combination - multiplex na reagents
- Device class
- Class IVD GeneralClass C
- EU registration type
- Legacy device (under a directive)Standard device
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000026452
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